Ventris Medical earned FDA 510(k) clearance for its Backpack bone graft containment system, according to a Jan. 9 news release.
Backpack is a porous biologic scaffold designed for orthopedic and spinal fusions. It is available in two versions - one prefilled with Allocell AF allograft fibers and one prefilled with surface activated amplify granules.
"The Backpack technology platform is our latest venture in enhancing the surgeon experience and fusion outcomes," John Brunelle, PhD, COO of Ventris Medical, said in the release. "The sophisticated design of the containment system allows for precise delivery and retention of our clinically validated biphasic granules and allograft fibers, ensuring a more consistent healing response at the fusion site. This latest milestone establishes yet another platform for future product developments and further validates Ventris as a key innovator in the orthobiologics space."